| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:63056743-63057135 | Common:3; Rare:85; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:63060797-63060952 | Rare:41; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr15:63062184-63062393 | Rare:50; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:63156411-63156770 | Common:1; Rare:91 | ||||
| chr15:63157402-63157555 | Common:2; Rare:67 | ||||
| chr15:63189316-63189678 | Common:2; Rare:115 | ||||
| chr15:63189745-63189831 | Rare:23 | ||||
| chr15:63277290-63277639 | Common:4; Rare:74 | ||||
| chr15:63504377-63504827 | Common:2; Rare:151 | ||||
| chr15:63505087-63505263 | Common:2; Rare:52 | ||||
| chr15:63553612-63553793 | Rare:26 | ||||
| chr15:63586645-63586749 | Common:2; Rare:12 | ||||
| chr15:63597200-63597429 | Common:1; Rare:66 | ||||
| chr15:63597528-63597612 | Rare:37 | ||||
| chr15:63833879-63834053 | Common:1; Rare:68 |